{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Gainesville",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90620",
      "recalling_firm": "Myolyn Inc.",
      "address_1": "6931 Nw 22nd St Ste A",
      "address_2": "",
      "postal_code": "32653-1231",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to AZ, CA, CT, FL, GA, ID, IL, KY, MA, MI, MN, MO, MN, NC, NJ, NM, NY, OH, OR, TX, UT, VA, WA, and WI.  There was no foreign/military/government distribution.",
      "recall_number": "Z-1523-2022",
      "product_description": "Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.",
      "product_quantity": "45 devices",
      "reason_for_recall": "Screws mounting an internal power supply may come loose during shipping resulting in increased risk of high voltage electrical shock.",
      "recall_initiation_date": "20220719",
      "center_classification_date": "20220816",
      "termination_date": "20240923",
      "report_date": "20220824",
      "code_info": "Serial numbers 000800 thru 000819, 000821 thru 000822, 000824 thru 000827, 000829 thru 000831, 000835, 000836, 000840 thru 000842, 000850 thru 000852, and 000857 thru 000859; UDI 000861553000417",
      "more_code_info": ""
    }
  ]
}